A citation-based method for searching scientific literature

Troels Askhøj Andersen, Karin de Linde Lind Troelsen, Lars Allan Larsen. Cell Mol Life Sci 2014
Times Cited: 110







List of co-cited articles
954 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Genetics of congenital heart disease: the glass half empty.
Akl C Fahed, Bruce D Gelb, J G Seidman, Christine E Seidman. Circ Res 2013
304
39

De novo mutations in histone-modifying genes in congenital heart disease.
Samir Zaidi, Murim Choi, Hiroko Wakimoto, Lijiang Ma, Jianming Jiang, John D Overton, Angela Romano-Adesman, Robert D Bjornson, Roger E Breitbart, Kerry K Brown,[...]. Nature 2013
517
31

Transcription factor pathways and congenital heart disease.
David J McCulley, Brian L Black. Curr Top Dev Biol 2012
181
27

De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies.
Jason Homsy, Samir Zaidi, Yufeng Shen, James S Ware, Kaitlin E Samocha, Konrad J Karczewski, Steven R DePalma, David McKean, Hiroko Wakimoto, Josh Gorham,[...]. Science 2015
331
23

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
Vidu Garg, Irfan S Kathiriya, Robert Barnes, Marie K Schluterman, Isabelle N King, Cheryl A Butler, Caryn R Rothrock, Reenu S Eapen, Kayoko Hirayama-Yamada, Kunitaka Joo,[...]. Nature 2003
797
21

The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
18

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.
Alejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, Jeroen Breckpot, Saeed H Al Turki, Bernard Thienpont, Jeremy McRae, Tomas W Fitzgerald, Tarjinder Singh, Ganesh Jawahar Swaminathan,[...]. Nat Genet 2016
154
17

Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.
Mary Ella Pierpont, Craig T Basson, D Woodrow Benson, Bruce D Gelb, Therese M Giglia, Elizabeth Goldmuntz, Glenn McGee, Craig A Sable, Deepak Srivastava, Catherine L Webb. Circulation 2007
527
16

Genetic basis of congenital cardiovascular malformations.
Seema R Lalani, John W Belmont. Eur J Med Genet 2014
44
36

Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis.
Denise van der Linde, Elisabeth E M Konings, Maarten A Slager, Maarten Witsenburg, Willem A Helbing, Johanna J M Takkenberg, Jolien W Roos-Hesselink. J Am Coll Cardiol 2011
16

Rare variants in NR2F2 cause congenital heart defects in humans.
Saeed Al Turki, Ashok K Manickaraj, Catherine L Mercer, Sebastian S Gerety, Marc-Phillip Hitz, Sarah Lindsay, Lisa C A D'Alessandro, G Jawahar Swaminathan, Jamie Bentham, Anne-Karin Arndt,[...]. Am J Hum Genet 2014
92
16

Congenital heart disease caused by mutations in the transcription factor NKX2-5.
J J Schott, D W Benson, C T Basson, W Pease, G M Silberbach, J P Moak, B J Maron, C E Seidman, J G Seidman. Science 1998
888
15

The changing epidemiology of congenital heart disease.
Teun van der Bom, A Carla Zomer, Aeilko H Zwinderman, Folkert J Meijboom, Berto J Bouma, Barbara J M Mulder. Nat Rev Cardiol 2011
318
14

Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy.
Edwin P Kirk, Margaret Sunde, Mauro W Costa, Scott A Rankin, Orit Wolstein, M Leticia Castro, Tanya L Butler, Changbaig Hyun, Guanglan Guo, Robyn Otway,[...]. Am J Hum Genet 2007
220
14

Global genetic analysis in mice unveils central role for cilia in congenital heart disease.
You Li, Nikolai T Klena, George C Gabriel, Xiaoqin Liu, Andrew J Kim, Kristi Lemke, Yu Chen, Bishwanath Chatterjee, William Devine, Rama Rao Damerla,[...]. Nature 2015
218
14

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
Rachel Soemedi, Ian J Wilson, Jamie Bentham, Rebecca Darlay, Ana Töpf, Diana Zelenika, Catherine Cosgrove, Kerry Setchfield, Chris Thornborough, Javier Granados-Riveron,[...]. Am J Hum Genet 2012
180
13

GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve.
Lin-Mei Shi, Ju-Wei Tao, Xing-Biao Qiu, Juan Wang, Fang Yuan, Lei Xu, Hua Liu, Ruo-Gu Li, Ying-Jia Xu, Qian Wang,[...]. Int J Mol Med 2014
56
21

Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.
Joseph T Glessner, Alexander G Bick, Kaoru Ito, Jason Homsy, Laura Rodriguez-Murillo, Menachem Fromer, Erica Mazaika, Badri Vardarajan, Michael Italia, Jeremy Leipzig,[...]. Circ Res 2014
128
12

TBX20 loss-of-function mutation contributes to double outlet right ventricle.
Yun Pan, Rui Geng, Ning Zhou, Gui-Fen Zheng, Hong Zhao, Juan Wang, Cui-Mei Zhao, Xing-Biao Qiu, Yi-Qing Yang, Xing-Yuan Liu. Int J Mol Med 2015
24
50

A novel mutation of GATA4 (K300T) associated with familial atrial septal defect.
Jia Chen, Bingyang Qi, Juan Zhao, Wei Liu, Ranhui Duan, Mingqiu Zhang. Gene 2016
25
48

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Sheng Chih Jin, Jason Homsy, Samir Zaidi, Qiongshi Lu, Sarah Morton, Steven R DePalma, Xue Zeng, Hongjian Qi, Weni Chang, Michael C Sierant,[...]. Nat Genet 2017
260
12

Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.
Kathy J Jenkins, Adolfo Correa, Jeffrey A Feinstein, Lorenzo Botto, Amy E Britt, Stephen R Daniels, Marsha Elixson, Carole A Warnes, Catherine L Webb. Circulation 2007
455
11

PITX2 loss-of-function mutation contributes to tetralogy of Fallot.
Yu-Min Sun, Jun Wang, Xing-Biao Qiu, Fang Yuan, Ying-Jia Xu, Ruo-Gu Li, Xin-Kai Qu, Ri-Tai Huang, Song Xue, Yi-Qing Yang. Gene 2016
23
47

De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.
James R Priest, Kazutoyo Osoegawa, Nebil Mohammed, Vivek Nanda, Ramendra Kundu, Kathleen Schultz, Edward J Lammer, Santhosh Girirajan, Todd Scheetz, Daryl Waggott,[...]. PLoS Genet 2016
58
18

A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease.
Yun Pan, Zha-Gen Wang, Xing-Yuan Liu, Hong Zhao, Ning Zhou, Gui-Fen Zheng, Xing-Biao Qiu, Ruo-Gu Li, Fang Yuan, Hong-Yu Shi,[...]. Pediatr Cardiol 2015
23
47

A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.
Yu-Min Sun, Jun Wang, Xing-Biao Qiu, Fang Yuan, Ruo-Gu Li, Ying-Jia Xu, Xin-Kai Qu, Hong-Yu Shi, Xu-Min Hou, Ri-Tai Huang,[...]. G3 (Bethesda) 2016
26
42

A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot.
Cai-Xia Lu, Hai-Rong Gong, Xing-Yuan Liu, Juan Wang, Cui-Mei Zhao, Ri-Tai Huang, Song Xue, Yi-Qing Yang. Int J Mol Med 2016
31
35

Genetics and Genomics of Congenital Heart Disease.
Samir Zaidi, Martina Brueckner. Circ Res 2017
140
11

Somatic GATA5 mutations in sporadic tetralogy of Fallot.
Ri-Tai Huang, Song Xue, Ying-Jia Xu, Min Zhou, Yi-Qing Yang. Int J Mol Med 2014
20
50

A novel mutation of GATA4 (K319E) is responsible for familial atrial septal defect and pulmonary valve stenosis.
Rong Xiang, Liang-Liang Fan, Hao Huang, Bei-Bei Cao, Xiang-Ping Li, Dao-Quan Peng, Kun Xia. Gene 2014
40
25

GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect.
Dong Wei, Han Bao, Ning Zhou, Gui-Fen Zheng, Xing-Yuan Liu, Yi-Qing Yang. Pediatr Cardiol 2013
34
29

Mechanisms of T-box gene function in the developing heart.
Franziska Greulich, Carsten Rudat, Andreas Kispert. Cardiovasc Res 2011
149
10

The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease.
Dorothy Warburton, Michael Ronemus, Jennie Kline, Vaidehi Jobanputra, Ismee Williams, Kwame Anyane-Yeboa, Wendy Chung, Lan Yu, Nancy Wong, Danielle Awad,[...]. Hum Genet 2014
78
12

Recurrence of congenital heart defects in families.
Nina Øyen, Gry Poulsen, Heather A Boyd, Jan Wohlfahrt, Peter K A Jensen, Mads Melbye. Circulation 2009
182
10

Lifetime prevalence of congenital heart disease in the general population from 2000 to 2010.
Ariane J Marelli, Raluca Ionescu-Ittu, Andrew S Mackie, Liming Guo, Nandini Dendukuri, Mohammed Kaouache. Circulation 2014
504
10


Genetic variations of NKX2-5 in sporadic atrial septal defect and ventricular septal defect in Chinese Yunnan population.
Yu Cao, Junqiang Wang, Chuanyu Wei, Zongliu Hou, Yaxiong Li, Honglin Zou, Mingyao Meng, Wenju Wang, Lihong Jiang. Gene 2016
22
45

MESP1 Mutations in Patients with Congenital Heart Defects.
Petra Werner, Brande Latney, Matthew A Deardorff, Elizabeth Goldmuntz. Hum Mutat 2016
22
45

A novel NKX2.6 mutation associated with congenital ventricular septal defect.
Juan Wang, Jian-Hui Mao, Ke-Ke Ding, Wei-Jun Xu, Xing-Yuan Liu, Xing-Biao Qiu, Ruo-Gu Li, Xin-Kai Qu, Ying-Jia Xu, Ri-Tai Huang,[...]. Pediatr Cardiol 2015
18
55

Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature.
Sabrina Gade Ellesøe, Morten Munk Johansen, Jesper Vandborg Bjerre, Vibeke Elisabeth Hjortdal, Søren Brunak, Lars Allan Larsen. Congenit Heart Dis 2016
42
23

Advances in the Genetics of Congenital Heart Disease: A Clinician's Guide.
Gillian M Blue, Edwin P Kirk, Eleni Giannoulatou, Gary F Sholler, Sally L Dunwoodie, Richard P Harvey, David S Winlaw. J Am Coll Cardiol 2017
56
17

GATA4 loss-of-function mutations underlie familial tetralogy of fallot.
Yi-Qing Yang, Lara Gharibeh, Ruo-Gu Li, Yuan-Feng Xin, Juan Wang, Zhong-Min Liu, Xing-Biao Qiu, Ying-Jia Xu, Lei Xu, Xin-Kai Qu,[...]. Hum Mutat 2013
47
19

Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
Dong Wei, Xiao-Hui Gong, Gang Qiu, Juan Wang, Yi-Qing Yang. Int J Mol Med 2014
24
37

Genetic and functional analyses of ZIC3 variants in congenital heart disease.
Jason Cowan, Muhammad Tariq, Stephanie M Ware. Hum Mutat 2014
36
25

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
Steven C Greenway, Alexandre C Pereira, Jennifer C Lin, Steven R DePalma, Samuel J Israel, Sonia M Mesquita, Emel Ergul, Jessie H Conta, Joshua M Korn, Steven A McCarroll,[...]. Nat Genet 2009
296
9

A novel NKX2.5 loss-of-function mutation associated with congenital bicuspid aortic valve.
Xin-Kai Qu, Xing-Biao Qiu, Fang Yuan, Juan Wang, Cui-Mei Zhao, Xing-Yuan Liu, Xian-Ling Zhang, Ruo-Gu Li, Ying-Jia Xu, Xu-Min Hou,[...]. Am J Cardiol 2014
51
17

Heart disease and stroke statistics--2015 update: a report from the American Heart Association.
Dariush Mozaffarian, Emelia J Benjamin, Alan S Go, Donna K Arnett, Michael J Blaha, Mary Cushman, Sarah de Ferranti, Jean-Pierre Després, Heather J Fullerton, Virginia J Howard,[...]. Circulation 2015
9

Genetics of congenital heart disease: the contribution of the noncoding regulatory genome.
Alex V Postma, Connie R Bezzina, Vincent M Christoffels. J Hum Genet 2016
35
25


Genetic mutation analysis in Japanese patients with non-syndromic congenital heart disease.
Akiko Yoshida, Hiroko Morisaki, Mai Nakaji, Masataka Kitano, Ki-Sung Kim, Koichi Sagawa, Shiro Ishikawa, Ichiro Satokata, Yoshihide Mitani, Hitoshi Kato,[...]. J Hum Genet 2016
21
42


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.